Written | 08-2018 | Jean-Loup Huret, Philippe Dessen |
Identity |
Atlas_Id | 101186 |
Phylum | Lung, Heart, Skin, Other: Lung:: |
WHO/OMS Classification | Lung, Heart, Skin, Other |
Note | Non-annotated chromosomal abnormality. Preliminary data : if you are an author who wish to write a full paper/card on this translocation, go to How to contribute |
Clinics and Pathology |
Disease | Lung: Nonneoplastic epithelial disorder/lesion |
Genes involved and Proteins |
Gene Name | SCNN1A |
Location | 12p13.31 |
Gene Name | TNFRSF1A |
Location | 12p13.31 |
Bibliography |
Recurrent chimeric fusion RNAs in non-cancer tissues and cells |
Babiceanu M, Qin F, Xie Z, Jia Y, Lopez K, Janus N, Facemire L, Kumar S, Pang Y, Qi Y, Lazar IM, Li H |
Nucleic Acids Res 2016 Apr 7;44(6):2859-72 |
PMID 26837576 |
Read-through transcripts in normal human lung parenchyma are down-regulated in lung adenocarcinoma |
Pintarelli G, Dassano A, Cotroneo CE, Galvan A, Noci S, Piazza R, Pirola A, Spinelli R, Incarbone M, Palleschi A, Rosso L, Santambrogio L, Dragani TA, Colombo F |
Oncotarget 2016 May 10;7(19):27889-98 |
PMID 27058892 |
Translocations implicated (Data extracted from papers in the Atlas) |
t(12;12)(p13;p13) SCNN1A/TNFRSF1A | |
External links |
REVIEW articles | automatic search in PubMed |
Last year articles | automatic search in PubMed |
© Atlas of Genetics and Cytogenetics in Oncology and Haematology | indexed on : Thu Feb 14 18:07:29 CET 2019 |
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